Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis. [electronic resource]
Producer: 20161213Description: 1489-500 p. digitalISSN:- 1460-2083
- Antiporters
- Cation Transport Proteins
- Congenital Disorders of Glycosylation -- genetics
- Fungal Proteins -- genetics
- Glycosylation -- drug effects
- Golgi Apparatus -- drug effects
- HEK293 Cells
- HeLa Cells
- Homeostasis
- Humans
- Manganese -- metabolism
- Membrane Proteins -- deficiency
- Mutation
- Vesicular Transport Proteins -- metabolism
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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